• Product name

  • Description

    Rabbit polyclonal to MT-ND1
  • Host species

  • Tested applications

    Suitable for: IHC-P, WBmore details
  • Species reactivity

    Reacts with: Human, Pig
  • Immunogen

    Recombinant fragment corresponding to Human MT-ND1 aa 186-270. Two N-terminal tags, His-tag and GST-tag. Expressed in E.coli.


    Database link: P03886

  • Positive control

    • IHC-P: Human liver tissue. WB: Recombinant human MT-ND1 protein; Pig liver tissue lysate.



Our Abpromise guarantee covers the use of ab233289 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Application Abreviews Notes
IHC-P Use a concentration of 5 - 20 µg/ml.
WB Use a concentration of 0.2 - 2 µg/ml.


  • Function

    Core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) that is believed to belong to the minimal assembly required for catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone.
  • Involvement in disease

    Defects in MT-ND1 are a cause of Leber hereditary optic neuropathy (LHON) [MIM:535000]. LHON is a maternally inherited disease resulting in acute or subacute loss of central vision, due to optic nerve dysfunction. Cardiac conduction defects and neurological defects have also been described in some patients. LHON results from primary mitochondrial DNA mutations affecting the respiratory chain complexes.
    Defects in MT-ND1 are a cause of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome (MELAS) [MIM:540000]. MELAS is a genetically heterogenious disorder, characterized by episodic vomiting, seizures, and recurrent cerebral insults resembling strokes and causing hemiparesis, hemianopsia, or cortical blindness.
    Defects in MT-ND1 may be associated with susceptibility to Alzheimer disease mitochondrial (AD-MT) [MIM:502500]. Alzheimer disease is a neurodegenerative disorder characterized by progressive dementia, loss of cognitive abilities, and deposition of fibrillar amyloid proteins as intraneuronal neurofibrillary tangles, extracellular amyloid plaques and vascular amyloid deposits. The major constituent of these plaques is the neurotoxic amyloid-beta-APP 40-42 peptide (s), derived proteolytically from the transmembrane precursor protein APP by sequential secretase processing. The cytotoxic C-terminal fragments (CTFs) and the caspase-cleaved products such as C31 derived from APP, are also implicated in neuronal death.
    Defects in MT-ND1 may be associated with non-insulin-dependent diabetes mellitus (NIDDM).
  • Sequence similarities

    Belongs to the complex I subunit 1 family.
  • Cellular localization

    Mitochondrion inner membrane.
  • Information by UniProt
  • Database links

  • Alternative names

    • Complex I, subunit ND1 antibody
    • Mitochondrially encoded NADH dehydrogenase 1 antibody
    • MT-ND1 antibody
    • MTND1 antibody
    • NAD1 antibody
    • NADH dehydrogenase subunit 1 (complex I) antibody
    • NADH dehydrogenase subunit 1 antibody
    • NADH-ubiquinone oxidoreductase chain 1 antibody
    • NADH-ubiquinone oxidoreductase, subunit ND1 antibody
    • NADH1 antibody
    • ND1 antibody
    • NU1M_HUMAN antibody
    see all


  • Anti-MT-ND1 antibody (ab233289) at 3 µg/ml + Pig liver tissue lysate

    HRP-Linked Goat anti-Rabbit IgG polyclonal at 0.2 µg/ml
  • Formalin-fixed, paraffin-embedded human liver tissue stained for MT-ND1 using ab233289 at 10 µg/mL in immunohistochemical analysis. DAB staining.

  • Formalin-fixed, paraffin-embedded human kidney tissue stained for MT-ND1 using ab233289 at 20 µg/mL in immunohistochemical analysis. DAB staining.

  • Anti-MT-ND1 antibody (ab233289) at 2 µg/ml + Recombinant human MT-ND1 protein


ab233289 has not yet been referenced specifically in any publications.

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